Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP687195.RAfaOzw5TNmxKHVDwGRLQ4GJ-T5v0s6tjALEKRiz0bFuY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP687195.RAfaOzw5TNmxKHVDwGRLQ4GJ-T5v0s6tjALEKRiz0bFuY130_assertion type Assertion NP687195.RAfaOzw5TNmxKHVDwGRLQ4GJ-T5v0s6tjALEKRiz0bFuY130_head.
- NP687195.RAfaOzw5TNmxKHVDwGRLQ4GJ-T5v0s6tjALEKRiz0bFuY130_assertion description "[Overlaps between the diverse disorders were seen also for the JAK2V617F (MPN 66/89; 74%; MDS/MPN 4/14; 29%; MDS 2/63; 3%) and NRAS mutations (MDS 2/67; 3%; MPN 2/4; MDS/MPN 1/1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP687195.RAfaOzw5TNmxKHVDwGRLQ4GJ-T5v0s6tjALEKRiz0bFuY130_provenance.
- NP687195.RAfaOzw5TNmxKHVDwGRLQ4GJ-T5v0s6tjALEKRiz0bFuY130_assertion evidence source_evidence_literature NP687195.RAfaOzw5TNmxKHVDwGRLQ4GJ-T5v0s6tjALEKRiz0bFuY130_provenance.
- NP687195.RAfaOzw5TNmxKHVDwGRLQ4GJ-T5v0s6tjALEKRiz0bFuY130_assertion SIO_000772 19415278 NP687195.RAfaOzw5TNmxKHVDwGRLQ4GJ-T5v0s6tjALEKRiz0bFuY130_provenance.
- NP687195.RAfaOzw5TNmxKHVDwGRLQ4GJ-T5v0s6tjALEKRiz0bFuY130_assertion wasDerivedFrom befree-20140225 NP687195.RAfaOzw5TNmxKHVDwGRLQ4GJ-T5v0s6tjALEKRiz0bFuY130_provenance.
- NP687195.RAfaOzw5TNmxKHVDwGRLQ4GJ-T5v0s6tjALEKRiz0bFuY130_assertion wasGeneratedBy ECO_0000203 NP687195.RAfaOzw5TNmxKHVDwGRLQ4GJ-T5v0s6tjALEKRiz0bFuY130_provenance.